CA2260016C - Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2 - Google Patents

Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2 Download PDF

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CA2260016C
CA2260016C CA002260016A CA2260016A CA2260016C CA 2260016 C CA2260016 C CA 2260016C CA 002260016 A CA002260016 A CA 002260016A CA 2260016 A CA2260016 A CA 2260016A CA 2260016 C CA2260016 C CA 2260016C
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Prior art keywords
cox
compound
pyridine
phenyl
methylsulfonyl
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Expired - Lifetime
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CA002260016A
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CA2260016A1 (fr
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Daniel Dube
Rejean Fortin
Richard Friesen
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Merck Canada Inc
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Merck Frosst Canada and Co
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Priority claimed from GBGB9616126.0A external-priority patent/GB9616126D0/en
Priority claimed from GBGB9621420.0A external-priority patent/GB9621420D0/en
Priority claimed from GBGB9709291.0A external-priority patent/GB9709291D0/en
Application filed by Merck Frosst Canada and Co filed Critical Merck Frosst Canada and Co
Priority to CA2412968A priority Critical patent/CA2412968C/fr
Publication of CA2260016A1 publication Critical patent/CA2260016A1/fr
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D213/89Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom

Abstract

L'invention concerne le nouveau composé de la formule (I) de même qu'un procédé de traitement des maladies induites par COX-2, lequel consiste à administrer à un patient nécessitant un tel traitement une dose non toxique et efficace sur le plan thérapeutique d'un composé de la formule (I). L'invention concerne également certaines compositions pharmaceutiques destinées au traitement de maladies induites par COX-2, et comprenant les composés de la formule (I).
CA002260016A 1996-07-18 1997-07-08 Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2 Expired - Lifetime CA2260016C (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA2412968A CA2412968C (fr) 1996-07-18 1997-07-08 Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2

Applications Claiming Priority (11)

Application Number Priority Date Filing Date Title
US2212896P 1996-07-18 1996-07-18
US60/022,128 1996-07-18
GBGB9616126.0A GB9616126D0 (en) 1996-08-01 1996-08-01 Substituted pyridines as selective cyclooxygenase-2 inhibitors
GB9616126.0 1996-08-01
US2713996P 1996-10-01 1996-10-01
US60/027,139 1996-10-01
GBGB9621420.0A GB9621420D0 (en) 1996-10-15 1996-10-15 Substituted pyridines as selective cyclooxygenase-2 inhibitors
GB9621420.0 1996-10-15
US4181497P 1997-04-08 1997-04-08
GBGB9709291.0A GB9709291D0 (en) 1997-05-07 1997-05-07 Substituted pyridines as selective cyclooxygenase-2 inhibitors
PCT/CA1997/000486 WO1998003484A1 (fr) 1996-07-18 1997-07-08 Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2

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CA2412968A Division CA2412968C (fr) 1996-07-18 1997-07-08 Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2

Publications (2)

Publication Number Publication Date
CA2260016A1 CA2260016A1 (fr) 1998-01-29
CA2260016C true CA2260016C (fr) 2004-03-09

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CA002260016A Expired - Lifetime CA2260016C (fr) 1996-07-18 1997-07-08 Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2
CA2412968A Expired - Lifetime CA2412968C (fr) 1996-07-18 1997-07-08 Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2

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CA2412968A Expired - Lifetime CA2412968C (fr) 1996-07-18 1997-07-08 Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2

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EP (1) EP0912518B1 (fr)
JP (2) JP3251945B2 (fr)
KR (1) KR100371620B1 (fr)
CN (1) CN1152863C (fr)
AR (1) AR012825A1 (fr)
AT (1) ATE249437T1 (fr)
AU (1) AU723179B2 (fr)
BG (1) BG64553B1 (fr)
BR (1) BRPI9710372B8 (fr)
CA (2) CA2260016C (fr)
CO (1) CO4900063A1 (fr)
CY (1) CY2409B1 (fr)
CZ (1) CZ292843B6 (fr)
DE (1) DE69724788T2 (fr)
DK (1) DK0912518T3 (fr)
DZ (1) DZ2268A1 (fr)
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HK (1) HK1023767A1 (fr)
HR (1) HRP970389B1 (fr)
HU (1) HU227732B1 (fr)
ID (1) ID19602A (fr)
IL (1) IL127441A (fr)
IS (1) IS1958B (fr)
MY (1) MY134841A (fr)
NO (1) NO313327B1 (fr)
NZ (1) NZ333230A (fr)
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PT (1) PT912518E (fr)
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SI (1) SI0912518T1 (fr)
SK (1) SK283261B6 (fr)
TR (1) TR199900046T2 (fr)
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WO (1) WO1998003484A1 (fr)

Families Citing this family (93)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6512121B2 (en) 1998-09-14 2003-01-28 G.D. Searle & Co. Heterocyclo substituted hydroxamic acid derivatives as cyclooxygenase-2 and 5-lipoxygenase inhibitors
US6096753A (en) * 1996-12-05 2000-08-01 Amgen Inc. Substituted pyrimidinone and pyridone compounds and methods of use
ES2224366T3 (es) * 1997-03-14 2005-03-01 MERCK FROSST CANADA & CO. Piridazinonas como inhibidores de ciclooxigenasa-2.
US6004960A (en) * 1997-03-14 1999-12-21 Merck Frosst Canada, Inc. Pyridazinones as inhibitors of cyclooxygenase-2
US6127545A (en) * 1997-04-18 2000-10-03 Merck & Co., Inc. Process for making 2-aryl-3-aryl-5-halo pyridines useful as COX-2 inhibitors
US6130334A (en) * 1998-04-15 2000-10-10 Merck & Co., Inc. Process for making 2-aryl-3-aryl-5-halo pyridines useful as COX-2 inhibitors
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